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二酰基甘油激酶ζ对巨吞饮作用的调节

Regulation of Macropinocytosis by Diacylglycerol Kinase ζ.

作者信息

Ard Ryan, Mulatz Kirk, Pomoransky Julia L, Parks Robin J, Trinkle-Mulcahy Laura, Bell John C, Gee Stephen H

机构信息

Department of Cellular and Molecular Medicine, University of Ottawa, 451 Smyth Rd, Ottawa, ON, K1H 8M5, Canada.

Centre for Neuromuscular Disease, University of Ottawa, Ottawa, ON, Canada.

出版信息

PLoS One. 2015 Dec 23;10(12):e0144942. doi: 10.1371/journal.pone.0144942. eCollection 2015.

Abstract

Macropinosomes arise from the closure of plasma membrane ruffles to bring about the non-selective uptake of nutrients and solutes into cells. The morphological changes underlying ruffle formation and macropinosome biogenesis are driven by actin cytoskeleton rearrangements under the control of the Rho GTPase Rac1. We showed previously that Rac1 is activated by diacylglycerol kinase ζ (DGKζ), which phosphorylates diacylglycerol to yield phosphatidic acid. Here, we show DGKζ is required for optimal macropinocytosis induced by growth factor stimulation of mouse embryonic fibroblasts. Time-lapse imaging of live cells and quantitative analysis revealed DGKζ was associated with membrane ruffles and nascent macropinosomes. Macropinocytosis was attenuated in DGKζ-null cells, as determined by live imaging and vaccinia virus uptake experiments. Moreover, macropinosomes that did form in DGKζ-null cells were smaller than those found in wild type cells. Rescue of this defect required DGKζ catalytic activity, consistent with it also being required for Rac1 activation. A constitutively membrane bound DGKζ mutant substantially increased the size of macropinosomes and potentiated the effect of a constitutively active Rac1 mutant on macropinocytosis. Collectively, our results suggest DGKζ functions in concert with Rac1 to regulate macropinocytosis.

摘要

巨胞饮体源自质膜褶皱的闭合,从而实现细胞对营养物质和溶质的非选择性摄取。褶皱形成和巨胞饮体生物发生的形态学变化是由Rho GTP酶Rac1控制下的肌动蛋白细胞骨架重排驱动的。我们之前表明,Rac1被二酰基甘油激酶ζ(DGKζ)激活,该酶将二酰基甘油磷酸化生成磷脂酸。在此,我们表明DGKζ是小鼠胚胎成纤维细胞生长因子刺激诱导的最佳巨胞饮作用所必需的。活细胞的延时成像和定量分析表明,DGKζ与膜褶皱和新生巨胞饮体相关。通过活细胞成像和痘苗病毒摄取实验确定,DGKζ基因敲除细胞中的巨胞饮作用减弱。此外,DGKζ基因敲除细胞中形成的巨胞饮体比野生型细胞中的更小。这种缺陷的挽救需要DGKζ的催化活性,这与其对Rac1激活也是必需的一致。一种组成型膜结合DGKζ突变体显著增加了巨胞饮体的大小,并增强了组成型活性Rac1突变体对巨胞饮作用的影响。总之,我们的结果表明DGKζ与Rac1协同作用来调节巨胞饮作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04a2/4689489/6e3eb81747ea/pone.0144942.g001.jpg

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